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Drug Safety Regulatory Requirements


Overview

This module provides information about pharmacovigilance harmonization initiatives and regulatory requirements around world. It covers the key US and EU regulations, the roles that ICH and CIOMS play in drug safety regulations, good clinical and pharmacovigilance practices, and standard operating procedures (SOPs) that support drug safety.


“Excellent module! Well organized and explained. I loved the interactive elements included to entertain and reinforce learning!”  

-Previous Participant


Featured topics

  • Harmonization Initiatives
  • Important US Regulations
  • Important EU Regulations
  • 2010 EU Legislation
  • Global Safety Regulatory Resources
  • Good Pharmacovigilance Practices: Documentation
  • Standard Operating Procedures

Who should attend?

This module is designed for professionals involved in:

  • Drug safety and pharmacovigilance
  • Clinical research and development
  • Quality assurance and compliance
  • Regulatory affairs
  • Medical affairs
  • Marketing

Learning objectives

Upon completion of this module, learners should be able to:

  • Identify key harmonization initiatives involved in drug safety
  • Identify important US regulations
  • Identify important EU regulations
  • Describe the roles that the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) and Council for International Organizations of Medical Sciences (CIOMS) play in drug safety regulations
  • Describe good clinical and pharmacovigilance practices
  • Describe standard operating procedures (SOPs) that support drug safety

This module takes an average of 4 hours to complete.

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